Chemical Properties of 5H-4,1-benzoxazepine-2,5-dione,1,2-dihydro-1-methyl- (CAS 3455-21-8)

5H-4,1-benzoxazepine-2,5-dione,1,2-dihydro-1-methyl-

InChI
InChI=1S/C10H9NO3/c1-11-8-5-3-2-4-7(8)10(13)14-6-9(11)12/h2-5H,6H2,1H3
InChI Key
DTWXADABYFWAHU-UHFFFAOYSA-N
Formula
C10H9NO3
SMILES
CN1C(=O)COC(=O)c2ccccc21
Molecular Weight1
191.18
CAS
3455-21-8
Other Names
  • 5H-4,1-benoxazepine-2,5-dione,1,2-dihydro-1-methyl
Cheméo is a service of Céondo GmbH, since 2007, we provide simulation, modelling and software development services for the industry. Do not hesitate to contact us for your projects.

Physical Properties

Property Value Unit Source
ω 0.5667 Relay (1.0) Calculated Property
ΔfG° -181.77 kJ/mol Relay (1.0-beta) Calculated Property
ΔfH°gas -360.38 kJ/mol Relay (1.0) Calculated Property
ΔvapH° 86.04 kJ/mol Relay (1.0) Calculated Property
IE 8.65 eV Relay (1.0) Calculated Property
log10WS -1.85 Relay (1.0) Calculated Property
logPoct/wat 0.820 Crippen Calculated Property
McVol 136.130 ml/mol McGowan Calculated Property
Pc 3744.81 kPa Relay (1.0-beta) Calculated Property
Tboil 609.53 K Relay (1.0) Calculated Property
Tc 872.08 K Relay (1.0) Calculated Property
Tfus 418.37 K Relay (1.0) Calculated Property
Vc 0.498 m3/kmol Relay (1.0) Calculated Property

Similar Compounds

Anthranilic acid, n-glycoloyl-n-methyl-. Benzoic acid, 2-di(3-methylbutyl)amino-, 3-methylbutyl ester. Tetrazepam M (hydroxy-), isomer 2, hydrolysis, acetylated. Lycoramine. Benzoic acid, 2-di(2-methylbutyl)amino-, 2-methylbutyl ester. Spiro[2H-1-benzopyran-2,2'-[2H]indole], 1',3'-dihydro-1',3',3'-trimethyl-6-nitro-. vasicinone. narwedine. 6H-Benzofuro[3a,3,2-ef][2]benzazepin-6-one, 4a,5,9,10,11,12-hexahydro-3-methoxy-11-methyl-, (4aS,8aS)-. Carteolol, PFB-TMS. Benazepril desethyl 3Me (Benazeprilate 3Me). Tetrazepam M (hydroxy-), isomer 3, hydrolysis, acetylated. Benzoic acid, 2-di(3-methylbutyl)amino-, methyl ester. Tetrazepam M (hydroxy-), isomer 1, hydrolysis, acetylated. Tinctorine.

Find more compounds similar to 5H-4,1-benzoxazepine-2,5-dione,1,2-dihydro-1-methyl-.

Sources

Note: Cheméo is only indexing the data, follow the source links to retrieve the latest data. The source is also providing more information like the publication year, authors and more. Take the time to validate and double check the source of the data.